ENST00000265104.5:c.9839C>T
MANE Select
|
ENSP00000265104.4:p.Ala3280Val
|
|
ENST00000681290.1:c.9794C>T
|
ENSP00000505288.1:p.Ala3265Val
|
|
ENST00000265104.4:c.9839C>T
|
ENSP00000265104.4:p.Ala3280Val
|
|
ENST00000504001.3:n.551C>T
|
|
|
NM_001369.2:c.9839C>T
|
NP_001360.1:p.Ala3280Val
|
|
XM_005248262.2:c.9794C>T
|
XP_005248319.1:p.Ala3265Val
|
|
XM_005248262.3:c.9947C>T
|
XP_005248319.2:p.Ala3316Val
|
|
XM_017009177.1:c.9947C>T
|
XP_016864666.1:p.Ala3316Val
|
|
XM_017009178.1:c.8852C>T
|
XP_016864667.1:p.Ala2951Val
|
|
XM_017009179.2:c.8852C>T
|
XP_016864668.1:p.Ala2951Val
|
|
XM_017009180.1:c.9947C>T
|
XP_016864669.1:p.Ala3316Val
|
|
XM_017009181.1:c.9947C>T
|
XP_016864670.1:p.Ala3316Val
|
|
XM_017009182.1:c.9947C>T
|
XP_016864671.1:p.Ala3316Val
|
|
XM_017009185.1:c.5036C>T
|
XP_016864674.1:p.Ala1679Val
|
|
XM_017009186.1:c.4589C>T
|
XP_016864675.1:p.Ala1530Val
|
|
XM_017009188.1:c.3926C>T
|
XP_016864677.1:p.Ala1309Val
|
|
XM_024454388.1:c.8852C>T
|
XP_024310156.1:p.Ala2951Val
|
|
XM_024454389.1:c.8441C>T
|
XP_024310157.1:p.Ala2814Val
|
|
NM_001369.3:c.9839C>T
MANE Select
|
NP_001360.1:p.Ala3280Val
|
|